A rare cause of congenital hypotonia and bulbar palsy: a case of brown-vialetto-van laere syndrome type 1 in infancy
- International Journal of Family & Community Medicine
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Wesley Alfredo Gawlinski de Arruda,<sup>1</sup> Daniela Rigo,<sup>2</sup> Lianna S Facco,<sup>3</sup> Helen Luiza Silvestrini,<sup>4</sup> Leandra de Oliveira Rigo<sup>5</sup>
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Keywords
brown-vialetto-van laere syndrome, congenital hypotonia, bulbar palsy, riboflavin, SLC52A3, case report
